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Neuroblastoma mRNAs predict outcome in children with stage 4 neuroblastoma: a European HR-NBL1/SIOPEN study
VF. Viprey, WM. Gregory, MV. Corrias, A. Tchirkov, K. Swerts, A. Vicha, S. Dallorso, P. Brock, R. Luksch, D. Valteau-Couanet, V. Papadakis, G. Laureys, AD. Pearson, R. Ladenstein, SA. Burchill,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 2004 do Před 1 rokem
Open Access Digital Library
od 1999-01-01
PubMed
24590653
DOI
10.1200/jco.2013.53.3604
Knihovny.cz E-zdroje
- MeSH
- cisplatina aplikace a dávkování MeSH
- cyklofosfamid aplikace a dávkování MeSH
- dítě MeSH
- etoposid aplikace a dávkování MeSH
- homeodoménové proteiny genetika MeSH
- indukční chemoterapie MeSH
- Kaplanův-Meierův odhad MeSH
- karboplatina aplikace a dávkování MeSH
- kojenec MeSH
- kostní dřeň metabolismus MeSH
- lidé MeSH
- messenger RNA krev MeSH
- míra přežití MeSH
- mladiství MeSH
- nádorové biomarkery krev metabolismus MeSH
- neuroblastom farmakoterapie genetika metabolismus MeSH
- neuropeptidy genetika MeSH
- počítačová simulace MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- prediktivní hodnota testů MeSH
- předškolní dítě MeSH
- přežití bez známek nemoci MeSH
- proporcionální rizikové modely MeSH
- proteiny asociované s mikrotubuly genetika MeSH
- protokoly protinádorové kombinované chemoterapie terapeutické užití MeSH
- transkripční faktory genetika MeSH
- tyrosin-3-monooxygenasa genetika MeSH
- vinkristin aplikace a dávkování MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
PURPOSE: To evaluate the hypothesis that detection of neuroblastoma mRNAs by reverse transcriptase quantitative polymerase chain reaction (RTqPCR) in peripheral blood (PB) and bone marrow aspirates (BM) from children with stage 4 neuroblastoma are clinically useful biomarkers of risk. METHODS: RTqPCR for paired-like homeobox 2b (PHOX2B), tyrosine hydroxylase (TH), and doublecortin (DCX) mRNA in PB and BM of children enrolled onto the High-Risk Neuroblastoma Trial-1 of the European Society of Pediatric Oncology Neuroblastoma Group (HR-NBL1/SIOPEN) was performed at diagnosis and after induction therapy. RESULTS: High levels of TH, PHOX2B, or DCX mRNA in PB or BM at diagnosis strongly predicted for worse event-free survival (EFS) and overall survival (OS) in a cohort of 290 children. After induction therapy, high levels of these mRNAs predicted worse EFS and OS in BM but not in PB. Combinations of mRNAs in BM did not add to the predictive power of any single mRNA. However, in the original (n = 182) and validation (n = 137) PB cohorts, high TH (log10TH > 0.8) or high PHOX2B (log10PHOX2B > 0.28) identify 19% of children as ultrahigh risk, with 5-year EFS and OS rates of 0%; OS rate was 25% (95% CI, 16% to 36%) and EFS rate was 38% (95% CI, 28% to 49%) in the remaining children. The magnitude of reduction in mRNA level between diagnosis and postinduction therapy in BM or PB was not of additional predictive value. CONCLUSION: High levels of TH and PHOX2B mRNA in PB at diagnosis objectively identify children with ultrahigh-risk disease who may benefit from novel treatment approaches. The level of TH, PHOX2B, and DCX mRNA in BM and/or PB at diagnosis might contribute to an algorithm to improve stratification of children for treatment.
Ales Vicha Charles University and University Hospital Motol Prague Czech Republic
Dominique Valteau Couanet Institut Gustave Roussy Villejuif France
Katrien Swerts and Genevieve Laureys University Hospital Ghent Ghent Belgium
Maria 5 Corrias and Sandro Dallorso Gaslini Institute Genoa
Penelope Brock Great Ormond Street Hospital London
Ruth Ladenstein Children's Cancer Research Institute St Anna Children's Hospital Vienna Austria
Vassilios Papadakis Agia Sofia Children's Hospital Athens Greece
Virginie F Viprey and Susan A Burchill Leeds Institute of Cancer and Pathology
Walter M Gregory Clinical Trials Research Unit University of Leeds Leeds
Citace poskytuje Crossref.org
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- $a Viprey, Virginie F $u Virginie F. Viprey and Susan A. Burchill, Leeds Institute of Cancer and Pathology; Walter M. Gregory, Clinical Trials Research Unit, University of Leeds, Leeds; Penelope Brock, Great Ormond Street Hospital, London; Andrew D. Pearson, Institute of Cancer Research/Royal Marsden National Health Service Foundation Trust, Sutton, United Kingdom; Maria V. Corrias and Sandro Dallorso, Gaslini Institute, Genoa; Roberto Luksch, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico, Istituto Nazionale dei Tumori, Milano, Italy; Andrei Tchirkov, Centre Hospitalier Universitaire Clermont-Ferrand and Clermont Université, Université d'Auvergne, Clermont-Ferrand; Dominique Valteau-Couanet, Institut Gustave Roussy, Villejuif, France; Katrien Swerts and Genevieve Laureys, University Hospital Ghent, Ghent, Belgium; Ales Vicha, Charles University and University Hospital Motol, Prague, Czech Republic; Vassilios Papadakis, Agia Sofia Children's Hospital, Athens, Greece; and Ruth Ladenstein, Children's Cancer Research Institute/St Anna Children's Hospital, Vienna, Austria.
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